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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The present protocol provides a detailed procedure for inducing subarachnoid hemorrhage in mice via autologous blood injection to the anterior circulation and measuring delayed cerebral vasospasm by vascular gel casting.

Abstract

Subarachnoid hemorrhage (SAH) is a devastating illness, and patients who survive are still at risk for long-term neurological deficits. Cerebral vasospasm is one of several contributing factors to morbidity and mortality after SAH. Preclinical animal models are essential resources to investigate pathophysiology and novel therapeutics. This protocol provides a two-phase method for both inducing SAH in mice and evaluating delayed cerebral vasospasm by measuring cerebral artery diameter. In the first step, an anterior circulation autologous blood injection method is used to reproduce the most common anatomical location of human non-traumatic SAH and reliably control the volume and distribution of hemorrhage. The duration of this procedure is approximately 20 min per animal. Next, on post-SAH day 5, the cerebral vasculature is fixed and casted using a gelatin-dye solution before removing the brain for imaging. Finally, the diameter of many cerebral arteries can be measured simultaneously using a variety of image analysis software platforms. These procedures are rigorous and reproducible while also offering a time- and resource-efficient method for studying the pathophysiology of SAH and cerebral vasospasm.

Introduction

The morbidity and mortality caused by subarachnoid hemorrhage (SAH) are staggering despite decades of research and a plethora of disappointing candidate therapeutics1,2,3,4,5,6. Delayed cerebral ischemia (DCI) is a fundamental cause of poor outcomes among SAH patients, yet is an incompletely understood pathophysiologically7,8,9. There are many contributing factors to DCI, includin....

Protocol

The present protocol was approved and performed in compliance with the institutional policy and guidelines of the University of Florida Institutional Animal Care and Use Committee (#201910613). The representative experiment was conducted consistently with ARRIVE guidelines21. Female C57BL/6J mice, 12-15-week-old, were used for the experiments; however, mice of any age, strain, or sex can be used. Mice were housed in ventilated cages on a 12 h/12 h light-dark cycle with ad libitum access t.......

Representative Results

One of the primary advantages of this SAH model is the low mortality. Perioperative mortality is less than 10% for the SAH procedure, and perioperative deaths from the sham procedure are very rare; mortality rates during our development of this protocol were 6.7% and 0%, respectively (Table 1). Perioperative deaths in this SAH model, similar to other methods of SAH induction, are typically due to brain herniation secondary to increased intracranial pressure12.

Discussion

This protocol is a two-phase procedure for inducing SAH in mice and measuring cerebral vasospasm. This procedure is rigorous and reproducible while also maintaining time and resource efficiency. There are several critical steps in this procedure that must be adhered to closely. First, the coordinates of blood injections are of vital importance. Even a slight error in the location of the burr hole can lead to excessive bleeding from the dural venous sinuses and/or unintended injury to the cerebral vessels when the needle .......

Acknowledgements

This work was supported with funding from the following grants and organizations: National Institutes of Health (R01-NS110710 to BLH), The Brain Aneurysm Foundation (BAF2021-1483561969 to WSD and BLH), the James and Brigitte Marino Family Professorship Endowment, the Christine Desmond Fund, the Eblen Research Endowment, and the St. George Family Fund.

....

Materials

NameCompanyCatalog NumberComments
1 qt plastic bagsZiploc
1.5 mm drill bitDremel106
1 mL insulin syringesThermoFisher ScientificBD 329461
23 G Luer-lock needleBeckton-Dickinson (BD)305145
4% paraformaldehydeElabscienceE-IR-R113
5% Povidone-Iodine SolutionPBS Animal Health11205Chlorhexadine may be used per institutional guidelines or investigator preference
5-0 monofilament sutureEthicon698H
Absorbent bench coveringThermoFisher Scientific22-131-401
Adjustable heating padThermotechS766D
Bone waxBraintree ScientificDYNJBW 26
Camera microscope mount adapterAmScopeCA-NIK-SLR
Digital cameraNikonAny high resolution digital camera will be sufficient; specific model up to investigator preference
Dissecting microscopeLeicaM60
Ear tagsKent ScientificINS1005-5LS
Electric hair trimmerKent ScientificCL7300-Kit
ForcepsRoboz SurgicalRS-5136
GelatinThermoFisher ScientificS25335
Hamilton syringe with 28 G needleHamilton Company80630
Handheld rotary toolDremelModel #4000
Image analysis softwareImagePro10.0.04Other software platforms (e.g. ImageJ, Orbit) may be sufficient
India ink dyeThermoFisher ScientificNC9903975
KetaminePatterson Veterinary07-893-6763
Luer-lock syringes (3, 5, & 10 mL)Beckton-Dickinson (BD)309657, 309646, 309604
MiceCharles River LaboratoryC57BL/6Genetically-modfied strains may be used per study design
Mouse brain frame matrixHarvard Apparatus51386
Needle driverRoboz SurgicalRS-7860
Opthalmic ointmentDechra17033-211-38
Paraffin wax paperStellar ScientificHS234526AParafilm or equivalent
Phosphate-buffered salineThermoFisher Scientific50488886
Ruler or other measurement standardHarvard Apparatus51386
ScalpelRoboz Surgical65-9843
ScissorsRoboz SurgicalRS-5882
Stereotaxic frame with syringe holderHarvard Apparatus75-1822
Sterile cotton-tipped applicatorsUlineS-18991
Sterile gauzeThermoFisher Scientific19-090-729
Sterile salinePatterson Veterinary07-869-6657
Sterile surgical glovesAD SurgicalA5CS-LTX65
Sterile surgical gownAD SurgicalGWN-D02-CS
Surgical microscopeWorld Precision InstrumentsPSMB5N
XylazinePatterson Veterinary07-893-8424

References

  1. Hop, J. W., Rinkel, G. J. E., Algra, A., Van Gijn, J. Case-fatality rates and functional outcome after subarachnoid hemorrhage: A systematic review. Stroke. 28 (3), 660-664 (1997).
  2. Lovelock, C. E., Rinkel, G. J. E., Rothwell, P. M.

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